DYSTROPHIE MYOTONIQUE DE STEINERT PDF

Le Registre Dystrophie Myotonique (Myotonic Dystrophy Family Registry, .. fait en Californie et au Minnesota sur la dystrophie myotonique de Steinert à la. La dystrophie myotonique de Steinert (DM) est la plus fréquente des affections musculaires héréditaires non liées au sexe (incidence 1/). Le gène a été. Douze observations de dystrophie myotonique à début néonatal sont presentées . Six de ces observations comportaient une défaillance respiratoire néonatale.

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Affections neurologiques, Mjotonique myotonique type 1, Fatigue, Maladies neuromusculaires, Psychologie. Technical advances in neonatal intensive care now allow CDM1 children to survive prolonged ventilation.

Contact Help Who are we? Physical, mental and subjective fatigues are well known different types of fatigue.

Contact Help Who are we? However, clinically, it seems inefficient to try to understand those concepts separately, since they are highly intricate.

Literature on fatigue showed how relevant this trouble could dysgrophie for a majority of patients; and also how specific fatigue could be in Steinert disease, compared to other neuromuscular pathologies: We have examined literature about other affections for which fatigue were richly documented.

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Personal information regarding our website’s visitors, including their identity, is confidential. Access to the PDF text. The infant was extubated after 2 months.

Personal information regarding our website’s visitors, including their identity, is confidential. You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used or stored, be corrected, clarified, updated or deleted. Congenital myotonic dystrophy type I in a very premature neonate: The signification of such ventilatory needs on patient outcome, particularly for motor handicaps, speech and language delay, and mental deficiency, remains uncertain.

You may thus request that your data, should it be inaccurate, incomplete, unclear, outdated, not be used dystorphie stored, be corrected, clarified, updated or deleted. The owners of this website hereby guarantee to respect the legal confidentiality conditions, applicable in France, and not to disclose this data to third parties.

If you want to subscribe to this journal, see myotlnique rates You can purchase this item in Pay Per View: Outline Masquer le plan. The potential impact of in vitro fertilization on disease expression may also be considered.

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Literature review and research perspectives. If you want to subscribe to this journal, see our rates You can purchase this item in Pay Per View: La maladie de Steinert: You can move this window by clicking on the wteinert.

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Thus, more than in any other muscular diseases, factors that are not purely physical seem to be involved in fatigue felt by patients eteinert Steinert disease. Access to the PDF text.

Top of the page – Article Outline. La fatigue dans la dystrophie myotonique de Steinert: Access to the text HTML.

Dystrophie Myotonique de Type 1 – Maladie de Steinert – Description

If you are a subscriber, please sign in ‘My Account’ at the top right of the screen. The case of a week-old premature female infant, conceived by in vitro fertilization, is reported. Ethical concertation about withdrawal or maintenance of intensive care was engaged, taking into account the prolonged ventilation, the degree of prematurity, and the parental wishes for maximum care.